Label-free protein quantification in freshly ejaculated versus post-mating spermatophores of the noble crayfish Astacus astacus
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25871631
DOI
10.1016/j.jprot.2015.04.004
PII: S1874-3919(15)00165-7
Knihovny.cz E-resources
- Keywords
- Alpha-2-macroglobulin, Hemocyanin, Histone, Ryanodine receptor, Sodium/hydrogen exchanger, Spermatozoon capacitation,
- MeSH
- alpha-Macroglobulins metabolism MeSH
- Chromatography, Liquid MeSH
- Hemocyanins metabolism MeSH
- Histones metabolism MeSH
- Mass Spectrometry MeSH
- Sperm Capacitation MeSH
- Sodium-Hydrogen Exchangers metabolism MeSH
- Proteomics methods MeSH
- Ryanodine Receptor Calcium Release Channel metabolism MeSH
- Astacoidea physiology MeSH
- Sex Factors MeSH
- Spermatogonia physiology MeSH
- Spermatozoa physiology MeSH
- Up-Regulation MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- alpha-Macroglobulins MeSH
- Hemocyanins MeSH
- Histones MeSH
- Sodium-Hydrogen Exchangers MeSH
- Ryanodine Receptor Calcium Release Channel MeSH
UNLABELLED: Crayfish spermatophores are deposited on the body surface of the female during mating and remain there for a period of time before fertilization ensues. Post-mating changes in protein expression level in the noble crayfish Astacus astacus spermatophore were quantified. In-gel digestion and high resolution mass spectrometry were used for label-free protein quantification. One hundred twelve proteins were identified in the spermatophore of noble crayfish. After 7 days of storage on the body of the female, 6 proteins were identified in the post-mating spermatophore that showed significant up-regulation and 4 significant down-regulations (p < 0.05, fold change ≥ 2). The highest rate of up-regulation was observed in sodium/hydrogen exchanger, which may indicate the importance of intracellular pH adjustment for final maturation of the crayfish spermatozoon. The highest rate of down-regulation was observed in histone H2A. This may increase chromatin flexibility and facilitate its transfer into the oocyte during fertilization. The vitellogenin protein was identified in the crayfish spermatophore and its level changed during storage on the body surface of female. Extensive proteomic modification of male gametes during storage on the body surface of the female suggests post-mating final maturation of the crayfish spermatozoon. BIOLOGICAL SIGNIFICANCE: Freshwater crayfish comprise a large and diverse group of ecologically and commercially important animals. Molecular studies of gametes in the crayfish can provide insight into the complex process of reproduction in this diverse group of animals. The results of such studies can be used for development of new techniques for artificial reproduction of these economically important species.
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